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rs1064795576

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome2
Position165297054
GeneSCN2A
is asnp
is mentioned by
dbSNPrs1064795576
dbSNP (old)rs1064795576
ClinGenrs1064795576
ebirs1064795576
HLIrs1064795576
Exacrs1064795576
Gnomadrs1064795576
Varsomers1064795576
Maprs1064795576
PheGenIrs1064795576
Biobankrs1064795576
1000 genomesrs1064795576
hgdprs1064795576
ensemblrs1064795576
gopubmedrs1064795576
geneviewrs1064795576
scholarrs1064795576
googlers1064795576
pharmgkbrs1064795576
gwascentralrs1064795576
openSNPrs1064795576
23andMers1064795576
23andMe allrs1064795576
SNPshotrs1064795576
SNPdbers1064795576
MSV3drs1064795576
GWAS Ctlgrs1064795576
Max Magnitude0
ClinVar
Risk rs1064795576(A;A)
Alt rs1064795576(A;A)
Reference Rs1064795576(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166153564G>A
CLNSRC
CLNACC RCV000484885.1,